Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia

Objective: Bovine viral diarrhea (BVD) disease is a viral infection in cows caused by a sin¬gle-stranded plus-sense RNA virus of the Pestivirus genus under the Flaviviridae family. The clini¬cal manifestation of BVD mainly includes diarrhea and immunosuppression, thereby exacerbating various respira...

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Main Authors: Khalid, Nurulhidayah, Arshad, Siti Suri, Degu, Nurhusien Yimer, Ramanoon, Siti Zubaidah, Sadiq, Mohammed Babatunde
Format: Article
Language:English
Published: Network for the Veterinarians of Bangladesh 2024
Online Access:http://psasir.upm.edu.my/id/eprint/112015/1/Article%20on%20Molecular%20BVDV_JAVAR-2024.pdf
http://psasir.upm.edu.my/id/eprint/112015/
https://www.ejmanager.com/mnstemps/39/39-1692322038.pdf?t=1726029393
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Institution: Universiti Putra Malaysia
Language: English
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spelling my.upm.eprints.1120152024-09-17T02:33:36Z http://psasir.upm.edu.my/id/eprint/112015/ Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia Khalid, Nurulhidayah Arshad, Siti Suri Degu, Nurhusien Yimer Ramanoon, Siti Zubaidah Sadiq, Mohammed Babatunde Objective: Bovine viral diarrhea (BVD) disease is a viral infection in cows caused by a sin¬gle-stranded plus-sense RNA virus of the Pestivirus genus under the Flaviviridae family. The clini¬cal manifestation of BVD mainly includes diarrhea and immunosuppression, thereby exacerbating various respiratory diseases. This study was conducted to detect and molecularly characterize the bovine viral diarrhea disease virus (BVDV) in cattle on selected farms in Selangor, Malaysia. Materials and Methods: A reverse transcription polymerase chain reaction (RT-PCR) was performed for antigen detection in 253 plasma samples collected from cows using a cross-sectional study design. We selected the 5 untranslated regions (5’-UTR) region and the E2 region to compare the genetic differences between the isolates. Results: One sample was found to be positive (1/253) following RT-PCR targeting the conserved 5’-UTR region of BVDV. Thus, BVDV antigen prevalence was 0.40% (95% confidence interval: 0.0%–2.2%). By targeting the hypervariable E2 region of the isolated virus, UPM/MAL/BVDV/D17, the virus was classified under the subgenotype BVDV-1a. Conclusion: BVDV is present and circulating on selected cattle farms in Selangor, Malaysia. Given the presence of BVDV in several subgenotypes, the screening of all incoming cattle at Malaysia’s border is pertinent to prevent the entry of other BVDV subgenotypes into the country. Network for the Veterinarians of Bangladesh 2024 Article PeerReviewed text en cc_by_4 http://psasir.upm.edu.my/id/eprint/112015/1/Article%20on%20Molecular%20BVDV_JAVAR-2024.pdf Khalid, Nurulhidayah and Arshad, Siti Suri and Degu, Nurhusien Yimer and Ramanoon, Siti Zubaidah and Sadiq, Mohammed Babatunde (2024) Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia. Journal of Advanced Veterinary and Animal Research, 11 (2). pp. 474-482. ISSN 2311-7710 https://www.ejmanager.com/mnstemps/39/39-1692322038.pdf?t=1726029393 10.5455/javar.2024.k797
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description Objective: Bovine viral diarrhea (BVD) disease is a viral infection in cows caused by a sin¬gle-stranded plus-sense RNA virus of the Pestivirus genus under the Flaviviridae family. The clini¬cal manifestation of BVD mainly includes diarrhea and immunosuppression, thereby exacerbating various respiratory diseases. This study was conducted to detect and molecularly characterize the bovine viral diarrhea disease virus (BVDV) in cattle on selected farms in Selangor, Malaysia. Materials and Methods: A reverse transcription polymerase chain reaction (RT-PCR) was performed for antigen detection in 253 plasma samples collected from cows using a cross-sectional study design. We selected the 5 untranslated regions (5’-UTR) region and the E2 region to compare the genetic differences between the isolates. Results: One sample was found to be positive (1/253) following RT-PCR targeting the conserved 5’-UTR region of BVDV. Thus, BVDV antigen prevalence was 0.40% (95% confidence interval: 0.0%–2.2%). By targeting the hypervariable E2 region of the isolated virus, UPM/MAL/BVDV/D17, the virus was classified under the subgenotype BVDV-1a. Conclusion: BVDV is present and circulating on selected cattle farms in Selangor, Malaysia. Given the presence of BVDV in several subgenotypes, the screening of all incoming cattle at Malaysia’s border is pertinent to prevent the entry of other BVDV subgenotypes into the country.
format Article
author Khalid, Nurulhidayah
Arshad, Siti Suri
Degu, Nurhusien Yimer
Ramanoon, Siti Zubaidah
Sadiq, Mohammed Babatunde
spellingShingle Khalid, Nurulhidayah
Arshad, Siti Suri
Degu, Nurhusien Yimer
Ramanoon, Siti Zubaidah
Sadiq, Mohammed Babatunde
Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia
author_facet Khalid, Nurulhidayah
Arshad, Siti Suri
Degu, Nurhusien Yimer
Ramanoon, Siti Zubaidah
Sadiq, Mohammed Babatunde
author_sort Khalid, Nurulhidayah
title Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia
title_short Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia
title_full Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia
title_fullStr Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia
title_full_unstemmed Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia
title_sort molecular detection and genotyping of bovine viral diarrhea virus in selangor, malaysia
publisher Network for the Veterinarians of Bangladesh
publishDate 2024
url http://psasir.upm.edu.my/id/eprint/112015/1/Article%20on%20Molecular%20BVDV_JAVAR-2024.pdf
http://psasir.upm.edu.my/id/eprint/112015/
https://www.ejmanager.com/mnstemps/39/39-1692322038.pdf?t=1726029393
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